Variant DetailsVariant: dgv1906n54 Internal ID | 20135330 | Landmark | | Location Information | | Cytoband | 11q11 | Allele length | Assembly | Allele length | hg38 | 120960 | hg19 | 120960 | hg18 | 120960 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv554813, nsv554804, nsv554802, nsv554812, nsv554902, nsv554811, nsv554810, nsv554835, nsv554901 | Samples | HGDP00143, HGDP00908, NINDS_116, HGDP00759, HGDP00511, NINDS_257, 1782681210_A, 1798860371_A, HGDP01047, 1782681144_A, HGDP00210, HGDP00226, HGDP01238, HGDP01241, HGDP00791, 1780862415_A, HGDP00881, HGDP00537, NINDS_247, 1780854100_A, HGDP00617, HGDP00525, HGDP00520, HGDP00057, 1782681378_A, NINDS_162, 1780862071_A, HGDP00674, HGDP00820, HGDP00775, HGDP01021, HGDP00532, NINDS_256, NINDS_42, HGDP00106, NINDS_31, 1787431166_A, HGDP00587, HGDP00082, HGDP01345, 1780862261_A, HGDP01331, HGDP01302, HGDP01359, HGDP01318, HGDP00552, HGDP00909, HGDP00157, 1780854533_A, HGDP00643, HGDP01322, HGDP01201, NINDS_131, NINDS_127, 1780862394_A, HGDP00564, HGDP01282 | Known Genes | OR4C11, OR4C16, 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) | dgv1906n54
| Frequency | Sample Size | 17421 | Observed Gain | 31 | Observed Loss | 121 | Observed Complex | 0 | Frequency | n/a |
|
|