Variant DetailsVariant: nsv552859Internal ID | 15993582 | Landmark | | Location Information | | Cytoband | 11p15.5 | Allele length | Assembly | Allele length | hg38 | 99599 | hg19 | 99599 | hg18 | 99599 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv1523n54 | Supporting Variants | nssv763554 | Samples | | Known Genes | C11orf35, CDHR5, DEAF1, DRD4, IRF7, LOC143666, MIR210, MIR210HG, PHRF1, RASSF7, SCT | 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) | nsv552859
| Frequency | Sample Size | 17421 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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