Variant DetailsVariant: nsv1016831Internal ID | 18759366 | Landmark | | Location Information | | Cytoband | 7q35 | Allele length | Assembly | Allele length | hg38 | 641558 | hg19 | 641558 | hg18 | 641558 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv3670419 | Samples | | Known Genes | ARHGEF34P, ARHGEF35, ARHGEF5, CTAGE4, CTAGE6, CTAGE8, FAM115A, FAM115C, LOC154761, OR2A1, OR2A12, OR2A14, OR2A2, OR2A20P, OR2A25, OR2A42, OR2A5, OR2A7, OR2A9P, OR2F1, OR2F2, OR6B1, RNU6-57P | 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) | nsv1016831
| Frequency | Sample Size | 29084 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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