Variant DetailsVariant: nsv566127Internal ID | 16006850 | Landmark | | Location Information | | Cytoband | 14q32.33 | Allele length | Assembly | Allele length | hg38 | 679 | hg19 | 679 | hg18 | 679 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv3968n54 | Supporting Variants | nssv834697, nssv834695, nssv834699, nssv834694, nssv834696, nssv834698 | Samples | | Known Genes | CEP170B | 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) | nsv566127
| Frequency | Sample Size | 17421 | Observed Gain | 5 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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