Variant DetailsVariant: nsv554902 Internal ID | 15995625 | Landmark | | Location Information | | Cytoband | 11q11 | Allele length | Assembly | Allele length | hg38 | 89768 | hg19 | 89768 | hg18 | 89768 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv1906n54 | Supporting Variants | nssv776513, nssv1175366, nssv776511, nssv1175379, nssv1175374, nssv1175370, nssv1175371, nssv1175368, nssv1175375, nssv776515, nssv776512, nssv1175369, nssv1175373, nssv1175367, nssv776507, nssv776514, nssv1175376, nssv1175377, nssv776508, nssv776510, nssv776509, nssv1175378, nssv1175365, nssv1175372 | Samples | NINDS_116, NINDS_257, 1798860371_A, 1782681144_A, HGDP00226, HGDP01241, 1780862415_A, HGDP00057, HGDP00674, HGDP00532, HGDP00082, 1780862261_A, HGDP01302, HGDP00552, HGDP01201 | 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) | nsv554902
| Frequency | Sample Size | 17421 | Observed Gain | 2 | Observed Loss | 22 | Observed Complex | 0 | Frequency | n/a |
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