Variant DetailsVariant: nsv1007219Internal ID | 18749750 | Landmark | | Location Information | | Cytoband | 1q44 | Allele length | Assembly | Allele length | hg38 | 96668 | hg19 | 96668 | hg18 | 96668 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv626n100 | Supporting Variants | nssv3705607, nssv3501454, nssv3705609, nssv3497338, nssv3484253, nssv3487551, nssv3705608 | Samples | | Known Genes | OR2T10, OR2T11, OR2T29, OR2T34, OR2T35 | Method | SNP array | Analysis | Affymetrix SNP array copy number analysis | Platform | Affymetrix SNP Array 6.0 | Comments | | Reference | Coe_et_al_2014 | Pubmed ID | 25217958 | Accession Number(s) | nsv1007219
| Frequency | Sample Size | 29084 | Observed Gain | 0 | Observed Loss | 7 | Observed Complex | 0 | Frequency | n/a |
|
|