Variant DetailsVariant: dgv5084n100Internal ID | 20156700 | Landmark | | Location Information | | Cytoband | 4p16.2 | Allele length | Assembly | Allele length | hg38 | 306501 | hg19 | 306501 | hg18 | 387604 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv1005566, nsv999919, nsv999754, nsv1005868, nsv1010973, nsv1013748, nsv1007135, nsv1009515, nsv1009901, nsv1004434, nsv1008883, nsv997656, nsv1007614, nsv998453, nsv1009623, nsv1002732, nsv1004915, nsv1012613, nsv1009122, nsv1007512 | Samples | | Known Genes | FAM86EP | 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) | dgv5084n100
| Frequency | Sample Size | 29084 | Observed Gain | 0 | Observed Loss | 27 | Observed Complex | 0 | Frequency | n/a |
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