Variant DetailsVariant: nsv586323Internal ID | 16027046 | Landmark | | Location Information | | Cytoband | 20q13.31 | Allele length | Assembly | Allele length | hg38 | 1462 | hg19 | 1462 | hg18 | 1462 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv7619n54 | Supporting Variants | nssv941697, nssv941700, nssv941695, nssv941691, nssv941698, nssv941692, nssv941699, nssv941696, nssv941694, nssv941693, nssv941690 | Samples | | Known Genes | CTCFL | 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) | nsv586323
| Frequency | Sample Size | 17421 | Observed Gain | 4 | Observed Loss | 7 | Observed Complex | 0 | Frequency | n/a |
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