Variant DetailsVariant: nsv570811Internal ID | 16011534 | Landmark | | Location Information | | Cytoband | 15q26.3 | Allele length | Assembly | Allele length | hg38 | 1176 | hg19 | 1176 | hg18 | 1176 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv4783n54 | Supporting Variants | nssv850986, nssv850977, nssv850987, nssv850984, nssv850979, nssv850978, nssv850976, nssv850983, nssv850981, nssv850975, nssv850988, nssv850982, nssv850980, nssv850985 | Samples | | Known Genes | ALDH1A3 | 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) | nsv570811
| Frequency | Sample Size | 17421 | Observed Gain | 13 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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