Variant DetailsVariant: dgv1909n54 Internal ID | 20135333 | Landmark | | Location Information | | Cytoband | 11q11 | Allele length | Assembly | Allele length | hg38 | 91116 | hg19 | 91116 | hg18 | 91116 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv554896, nsv554930, nsv554857, nsv554873, nsv554931, nsv554963, nsv554859, nsv554850, nsv554871, nsv554870, nsv554856, nsv554860, nsv554817, nsv554875, nsv554898, nsv554855, nsv554929, nsv554816, nsv554858, nsv554934, nsv554876, nsv554854, nsv554951, nsv554853, nsv554938, nsv554928, nsv554910, nsv554944, nsv554962, nsv554872, nsv554899, nsv554877, nsv554874, nsv554851, nsv554933, nsv554961, nsv554852, nsv554923, nsv554831, nsv554932 | Samples | HGDP00637, HGDP00047, NINDS_232 | 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) | dgv1909n54
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 327 | Observed Complex | 0 | Frequency | n/a |
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