Variant DetailsVariant: dgv4707n54Internal ID | 20138131 | Landmark | | Location Information | | Cytoband | 15q26.1 | Allele length | Assembly | Allele length | hg38 | 1179 | hg19 | 1179 | hg18 | 1179 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv570402, nsv570408, nsv570406, nsv570414, nsv570415, nsv570401, nsv570412, nsv570407, nsv570418, nsv570413 | Samples | | Known Genes | FURIN | Method | SNP array | Analysis | Illumina SNP array copy number analysis | Platform | Not reported | Comments | | Reference | Cooper_et_al_2011 | Pubmed ID | 21841781 | Accession Number(s) | dgv4707n54
| Frequency | Sample Size | 17421 | Observed Gain | 28 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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