Internal ID | 15703164 |
Landmark | |
Location Information | |
Cytoband | 10q23.33 |
Allele length | Assembly | Allele length | hg38 | 115921 | hg19 | 115921 | hg18 | 115921 |
|
Variant Type | CNV loss |
Copy Number | |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | |
Merged Status | S |
Merged Variants | nsv551954 |
Supporting Variants | |
Samples | |
Known Genes | CYP2C18 |
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) | nssv755894
|
Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
|