Variant DetailsVariant: nsv1044362Internal ID | 18786893 | Landmark | | Location Information | | Cytoband | 13q12.12 | Allele length | Assembly | Allele length | hg38 | 1366337 | hg19 | 1366336 | hg18 | 1366336 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv1615n100 | Supporting Variants | nssv3523150 | Samples | | Known Genes | ANKRD20A19P, C1QTNF9, C1QTNF9B, C1QTNF9B-AS1, LINC00327, MIPEP, MIR2276, SACS, SACS-AS1, SGCG, SPATA13, SPATA13-AS1, TNFRSF19 | 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) | nsv1044362
| Frequency | Sample Size | 29084 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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