Variant DetailsVariant: nsv611144Internal ID | 16051867 | Landmark | | Location Information | | Cytoband | 8p11.1 | Allele length | Assembly | Allele length | hg38 | 767067 | hg19 | 767067 | hg18 | 767067 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv12123n54 | Supporting Variants | nssv1156595, nssv1156598, nssv1156599, nssv1156597, nssv1156596 | Samples | HGDP00650, HGDP00694, HGDP00776, HGDP00608, 1780862177_A | Known Genes | HGSNAT, POTEA | 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) | nsv611144
| Frequency | Sample Size | 17421 | Observed Gain | 5 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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