Variant DetailsVariant: nsv1061241Internal ID | 18803772 | Landmark | | Location Information | | Cytoband | 22q13.1 | Allele length | Assembly | Allele length | hg38 | 23830 | hg19 | 23830 | hg18 | 23830 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv4569n100 | Supporting Variants | nssv3600897, nssv3600900, nssv3600904, nssv3600908, nssv3734214, nssv3600905, nssv3600911, nssv3600906, nssv3600907, nssv3600899, nssv3600902, nssv3734213, nssv3600901, nssv3734215, nssv3600896, nssv3600903, nssv3600909, nssv3600910, nssv3600898 | Samples | | Known Genes | APOBEC3A, APOBEC3A_B | 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) | nsv1061241
| Frequency | Sample Size | 29084 | Observed Gain | 0 | Observed Loss | 19 | Observed Complex | 0 | Frequency | n/a |
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