Variant DetailsVariant: dgv1908n54Internal ID | 20135332 | Landmark | | Location Information | | Cytoband | 11q11 | Allele length | Assembly | Allele length | hg38 | 130165 | hg19 | 130165 | hg18 | 130165 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv554904, nsv554906, nsv554814 | Samples | HGDP01296, HGDP01003 | 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) | dgv1908n54
| Frequency | Sample Size | 17421 | Observed Gain | 3 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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