Variant DetailsVariant: dgv4446n54Internal ID | 20137870 | Landmark | | Location Information | | Cytoband | 15q13.3 | Allele length | Assembly | Allele length | hg38 | 409854 | hg19 | 409854 | hg18 | 409854 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv568866, nsv568865, nsv568872 | Samples | | Known Genes | CHRNA7, GOLGA8K, GOLGA8O, LOC100996255, ULK4P1, ULK4P2, ULK4P3, WHAMMP1 | 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) | dgv4446n54
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 3 | Observed Complex | 0 | Frequency | n/a |
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