Variant DetailsVariant: nsv1045080Internal ID | 18787611 | Landmark | | Location Information | | Cytoband | 12q13.13 | Allele length | Assembly | Allele length | hg38 | 97077 | hg19 | 97077 | hg18 | 97077 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv1503n100 | Supporting Variants | nssv3523549, nssv3712465, nssv3712466, nssv3523548, nssv3523546, nssv3523545, nssv3523544, nssv3523550, nssv3523547, nssv3712467, nssv3523543 | Samples | | Known Genes | KRT83, KRT84, KRT85, KRT86 | 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) | nsv1045080
| Frequency | Sample Size | 29084 | Observed Gain | 11 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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