Variant DetailsVariant: nsv570402Internal ID | 16011125 | Landmark | | Location Information | | Cytoband | 15q26.1 | Allele length | Assembly | Allele length | hg38 | 1128 | hg19 | 1128 | hg18 | 1128 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv4707n54 | Supporting Variants | nssv848229, nssv848227, nssv848231, nssv848224, nssv848230, nssv848226, nssv848225, nssv848228 | 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) | nsv570402
| Frequency | Sample Size | 17421 | Observed Gain | 8 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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