Variant DetailsVariant: dgv5621n100Internal ID | 20157237 | Landmark | | Location Information | | Cytoband | 5p13.3 | Allele length | Assembly | Allele length | hg38 | 57276 | hg19 | 57276 | hg18 | 57276 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv1033885, nsv1022116, nsv1015763, nsv1024864, nsv1030952, nsv1021778, nsv1033996, nsv1030853, nsv1029185, nsv1017349, nsv1026909, nsv1028879 | Samples | | Known Genes | GOLPH3, PDZD2 | 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) | dgv5621n100
| Frequency | Sample Size | 29084 | Observed Gain | 311 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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