Variant DetailsVariant: nsv550000Internal ID | 15990723 | Landmark | | Location Information | | Cytoband | 10p13 | Allele length | Assembly | Allele length | hg38 | 105706 | hg19 | 105706 | hg18 | 105706 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv961n54 | Supporting Variants | nssv1174127, nssv1174126 | Samples | 1782681109_A, 1780862043_A | Known Genes | DCLRE1C, MEIG1 | 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) | nsv550000
| Frequency | Sample Size | 17421 | Observed Gain | 2 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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