Variant DetailsVariant: nsv610766Internal ID | 16051489 | Landmark | | Location Information | | Cytoband | 8p21.3 | Allele length | Assembly | Allele length | hg38 | 205294 | hg19 | 205296 | hg18 | 205295 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv12054n54 | Supporting Variants | nssv1107474 | Samples | | Known Genes | BMP1, DMTN, FAM160B2, FGF17, HR, LGI3, MIR320A, NUDT18, PHYHIP, POLR3D, REEP4, SFTPC | 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) | nsv610766
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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