Description:
                                                    
                                                    
                                                         
                                                            
                                                            TRANSLOCATED CHROMOSOME 
                                                            
                                                    
                                                 
                                                
                                                
                                                
                                                
                                             
                                         
                                     
                                    
                                        
                                            
                                            
                                            
                                            
                                                
                                                    
                                                        
                                                            
                                                            
                                                                
                                                                    
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                                                                            Repository
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                                                                            NIGMS Human Genetic Cell Repository
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	| Subcollection | 
	Chromosome Abnormalities DGAP dbGaP | 
 
                                                                
                                                                
                                                                
                                                                
	| Alternate IDs | 
	GM17022 [TRANSLOCATED CHROMOSOME] | 
 
                                                                
                                                                
                                                                
                                                                
                                                                    
                                                                        | 
                                                                            Cell Type
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                                                                            Fibroblast
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                                                                        | 
                                                                            Transformant
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                                                                            Untransformed
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                                                                        | 
                                                                            Race
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                                                                            Asiatic Indian
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                                                                        | 
                                                                            Relation to Proband
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                                                                            proband
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                                                                        | 
                                                                            Confirmation
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                                                                            Karyotypic analysis after cell line submission to CCR
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                                                                        | 
                                                                            ISCN
                                                                         | 
                                                                        
                                                                            46,XX,t(2;20)(p21;p13).arr Xq11.1q12(61865213-67040497)x2 hmz,Xq13.1q25(70313556-123199221)x2 hmz,2q24.2q24.3(162705510-168222414)x2 hmz,3q22.3q28(138718816-191702659)x2 hmz,5q35.1q35.3(169154846-180420866)x2 hmz,7p21.1p15.1(17511517-29911394)x2 hmz,10q22.3q23.31(80173558-92431009)x2 hmz,12p13.1q15(12833150-69574905)x2 hmz,12q22q24.22(92595142-116638283)x2 hmz,15q23q25.3(68155593-84802737)x2 hmz,16p13.3(26670-5546417)x2 hmz, 16p12.1p11.2(22747493-31380104)x2 hmz,16q11.2q13(45092477-56182731)x2 hmz,19p13.2q13.33(9667978-54493318)x2 hmz
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                                                                            Species
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                                                                            Homo sapiens
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                                                                        | 
                                                                            Common Name
                                                                         | 
                                                                        
                                                                            Human
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                                                                            Remarks
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	| Passage Frozen | 
	10 | 
 
	|   | 
 
                                                                
	| IDENTIFICATION OF SPECIES OF ORIGIN | 
	Species of Origin Confirmed by Chromosome Analysis | 
 
	|   | 
 
                                                                
                                                                
                                                                
                                                                
	| Cytogenetics | 
	Chromosome 2: TRANSLOCATION Breakpoint 2p21 t(2;20)2p21 | 
 
	 | 
	Chromosome 20: TRANSLOCATION Breakpoint 20p13 t(2;20)20p13 | 
 
                                                                
                                                                
                                                                
                                                             
                                                         
                                                     
                                                 
                                                
                                                    
                                                        
                                                            
                                                            
                                                            
                                                                
	| Remarks | 
	Asiatic Indian; de novo; has multiple congenital anomalies | 
 
                                                                
                                                             
                                                            
                                                            
                                                         
                                                     
                                                 
                                                
                                                    
                                                        
                                                            
                                                            
                                                            
                                                                
	| Tang Z, Berlin DS, Toji L, Toruner GA, Beiswanger C, Kulkarni S, Martin CL, Emanuel BS, Christman M, Gerry NP, A dynamic database of microarray-characterized cell lines with various cytogenetic and genomic backgrounds G3 (Bethesda, Md)3:1143-9 2013 | 
 
	| PubMed ID: 23665875 | 
 
                                                                
                                                             
                                                            
                                                         
                                                     
                                                 
                                                
                                                
                                                
                                                    
                                                        
                                                            
                                                            
                                                                
	| Passage Frozen | 
	10 | 
 
	| Split Ratio | 
	1:6 | 
 
	| Temperature | 
	37 C | 
 
	| Percent CO2 | 
	5% | 
 
	| Medium | 
	Ham's F12 with 2mM L-glutamine or equivalent | 
 
	| Serum | 
	15% fetal bovine serum Not inactivated           | 
 
	| Substrate | 
	None specified | 
 
	| Subcultivation Method | 
	trypsin-EDTA | 
 
	| Supplement | 
	- | 
 
                                                                
                                                                
                                                             
                                                         
                                                     
                                                 
                                             
                                         
                                     
                                 
                                
                             
                         
                     
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