Variant DetailsVariant: nsv571544Internal ID | 16012267 | Landmark | | Location Information | | Cytoband | 16p13.11 | Allele length | Assembly | Allele length | hg38 | 38343 | hg19 | 38343 | hg18 | 38343 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv4926n54 | Supporting Variants | nssv1150552, nssv1150551, nssv1150549, nssv1150550, nssv852821 | Samples | HGDP00907, HGDP00928, HGDP00906, HGDP01201 | Known Genes | FOPNL | 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) | nsv571544
| Frequency | Sample Size | 17421 | Observed Gain | 5 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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