Variant DetailsVariant: dgv1911n54Internal ID | 20135335 | Landmark | | Location Information | | Cytoband | 11q11 | Allele length | Assembly | Allele length | hg38 | 40776 | hg19 | 40776 | hg18 | 40776 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv554907, nsv554825, nsv554887, nsv554926, nsv554824, nsv554886, nsv554842, nsv554914 | Samples | | Known Genes | OR4C11, OR4P4 | 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) | dgv1911n54
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 18 | Observed Complex | 0 | Frequency | n/a |
|
|