Variant DetailsVariant: dgv3519n100Internal ID | 20155135 | Landmark | | Location Information | | Cytoband | 19q13.12 | Allele length | Assembly | Allele length | hg38 | 12776 | hg19 | 12776 | hg18 | 12776 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv1064016, nsv1063118, nsv1060131, nsv1065016, nsv1056634, nsv1065890, nsv1059785, nsv1058174, nsv1057640, nsv1056060 | Samples | | Known Genes | FFAR3 | 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) | dgv3519n100
| Frequency | Sample Size | 29084 | Observed Gain | 0 | Observed Loss | 61 | Observed Complex | 0 | Frequency | n/a |
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