Variant DetailsVariant: dgv1916n54Internal ID | 20135340 | Landmark | | Location Information | | Cytoband | 11q11 | Allele length | Assembly | Allele length | hg38 | 103106 | hg19 | 103106 | hg18 | 103106 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv554837, nsv554924, nsv554905, nsv554878, nsv554862, nsv554836, nsv554861, nsv554903, nsv554935 | Samples | 1780854537_A, HGDP00189 | Known Genes | OR4C11, OR4C6, OR4P4, OR4S2 | 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) | dgv1916n54
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 16 | Observed Complex | 0 | Frequency | n/a |
|
|