Variant DetailsVariant: dgv5062n100Internal ID | 20156678 | Landmark | | Location Information | | Cytoband | 4p16.3 | Allele length | Assembly | Allele length | hg38 | 45481 | hg19 | 45373 | hg18 | 45373 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv1004981, nsv1009127, nsv1011030, nsv1004445, nsv1014322, nsv1009854, nsv1011225, nsv999669 | Samples | | Known Genes | ZNF595, ZNF718 | 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) | dgv5062n100
| Frequency | Sample Size | 29084 | Observed Gain | 0 | Observed Loss | 9 | Observed Complex | 0 | Frequency | n/a |
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