Variant DetailsVariant: dgv4335n100Internal ID | 20155951 | Landmark | | Location Information | | Cytoband | 20q13.32 | Allele length | Assembly | Allele length | hg38 | 91792 | hg19 | 91792 | hg18 | 91792 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv1063880, nsv1059132, nsv1066293, nsv1060589, nsv1059035, nsv1060714, nsv1065560, nsv1062840, nsv1059752, nsv1061522, nsv1055705, nsv1056705, nsv1056600, nsv1058271, nsv1063750 | Samples | | Known Genes | FAM217B, PHACTR3, SYCP2 | 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) | dgv4335n100
| Frequency | Sample Size | 29084 | Observed Gain | 0 | Observed Loss | 22 | Observed Complex | 0 | Frequency | n/a |
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