Variant DetailsVariant: dgv3626n100Internal ID | 20155242 | Landmark | | Location Information | | Cytoband | 19q13.33 | Allele length | Assembly | Allele length | hg38 | 378712 | hg19 | 378712 | hg18 | 378712 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv1059924, nsv1057217, nsv1061029, nsv1062154, nsv1064732, nsv1057485, nsv1061100, nsv1056146, nsv1060988, nsv1063940, nsv1060519, nsv1059263, nsv1058292, nsv1057290 | Samples | | Known Genes | FPR1, FPR2, FPR3, HCCAT3, ZNF350, ZNF432, ZNF577, ZNF613, ZNF614, ZNF615, ZNF616, ZNF649, ZNF841 | 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) | dgv3626n100
| Frequency | Sample Size | 29084 | Observed Gain | 27 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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