Variant DetailsVariant: nsv546269Internal ID | 15986992 | Landmark | | Location Information | | Cytoband | 1p32.3 | Allele length | Assembly | Allele length | hg38 | 163896 | hg19 | 163896 | hg18 | 163896 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv1173856 | Samples | HGDP01101 | Known Genes | ACOT11, FAM151A, MROH7, MROH7-TTC4, PARS2, TTC4 | 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) | nsv546269
| Frequency | Sample Size | 17421 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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