Variant DetailsVariant: nsv615213Internal ID | 16055936 | Landmark | | Location Information | | Cytoband | 9q32 | Allele length | Assembly | Allele length | hg38 | 31054 | hg19 | 31054 | hg18 | 31054 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv1176139 | Samples | HGDP01171 | Known Genes | FKBP15, SLC31A2 | 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) | nsv615213
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
|
|