Variant DetailsVariant: dgv635n100Internal ID | 20152251 | Landmark | | Location Information | | Cytoband | 1q44 | Allele length | Assembly | Allele length | hg38 | 64899 | hg19 | 64899 | hg18 | 64899 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv1010035, nsv999467, nsv998342, nsv1011570, nsv1007075, nsv1007594, nsv1013857, nsv1008410, nsv1009248, nsv1003586, nsv997868, nsv1007867 | Samples | | Known Genes | OR2T10, OR2T11, OR2T27, 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) | dgv635n100
| Frequency | Sample Size | 29084 | Observed Gain | 0 | Observed Loss | 25 | Observed Complex | 0 | Frequency | n/a |
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