Variant DetailsVariant: nssv3584779Internal ID | 18536374 | Landmark | | Location Information | | Cytoband | 20q12 | Allele length | Assembly | Allele length | hg38 | 1992978 | hg19 | 1992978 | hg18 | 1992978 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv1064246 | Supporting Variants | | Samples | | Known Genes | CHD6, EMILIN3, LPIN3, MAFB, MIR6871, PLCG1, PTPRT, TOP1, ZHX3 | 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) | nssv3584779
| Frequency | Sample Size | 29084 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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