Variant DetailsVariant: nsv570403Internal ID | 16011126 | Landmark | | Location Information | | Cytoband | 15q26.1 | Allele length | Assembly | Allele length | hg38 | 1179 | hg19 | 1179 | hg18 | 1179 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv4708n54 | Supporting Variants | nssv848247, nssv848253, nssv848252, nssv848246, nssv848241, nssv848235, nssv848243, nssv848233, nssv848236, nssv848242, nssv848237, nssv848250, nssv848249, nssv848244, nssv848239, nssv848238, nssv848251, nssv848234, nssv848248, nssv848240, nssv848232, nssv848245 | 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) | nsv570403
| Frequency | Sample Size | 17421 | Observed Gain | 21 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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