Variant DetailsVariant: dgv1914n54Internal ID | 20135338 | Landmark | | Location Information | | Cytoband | 11q11 | Allele length | Assembly | Allele length | hg38 | 62548 | hg19 | 62548 | hg18 | 62548 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv554843, nsv554917, nsv554889, nsv554909, nsv554908, nsv554891, nsv554868, nsv554827, nsv554892, nsv554927, nsv554845, nsv554849, nsv554848, nsv554846, nsv554918, nsv554869, nsv554844, nsv554866, nsv554847, nsv554867, nsv554829, nsv554893, nsv554830, nsv554919 | Samples | | Known Genes | OR4C11, 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) | dgv1914n54
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 64 | Observed Complex | 0 | Frequency | n/a |
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