Internal ID | 15889392 |
Landmark | |
Location Information | |
Cytoband | 20q13.33 |
Allele length | Assembly | Allele length | hg38 | 69032 | hg19 | 69032 | hg18 | 69032 |
|
Variant Type | CNV loss |
Copy Number | |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | |
Merged Status | S |
Merged Variants | nsv586497 |
Supporting Variants | |
Samples | |
Known Genes | CABLES2, LAMA5, RBBP8NL, RPS21 |
Method | SNP array |
Analysis | Illumina SNP array copy number analysis |
Platform | Not reported |
Comments | |
Reference | Cooper_et_al_2011 |
Pubmed ID | 21841781 |
Accession Number(s) | nssv942122
|
Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
|