Variant DetailsVariant: nsv571527Internal ID | 16012250 | Landmark | | Location Information | | Cytoband | 16p13.11 | Allele length | Assembly | Allele length | hg38 | 43320 | hg19 | 43320 | hg18 | 43320 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv1150543, nssv852803, nssv1150545, nssv1150544 | Samples | 1780862015_A, 1782681079_A, HGDP00005 | Known Genes | NTAN1, PDXDC1, RRN3 | 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) | nsv571527
| Frequency | Sample Size | 17421 | Observed Gain | 2 | Observed Loss | 2 | Observed Complex | 0 | Frequency | n/a |
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