Variant DetailsVariant: nsv568777Internal ID | 16009500 | Landmark | | Location Information | | Cytoband | 15q13.3 | Allele length | Assembly | Allele length | hg38 | 2069 | hg19 | 2069 | hg18 | 2069 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv839508, nssv839510, nssv839506, nssv839509, nssv839507 | Samples | | Known Genes | KLF13 | 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) | nsv568777
| Frequency | Sample Size | 17421 | Observed Gain | 4 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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