Variant DetailsVariant: nsv516516Internal ID | 15097123 | Landmark | | Location Information | | Cytoband | 6q14.3 | Allele length | Assembly | Allele length | hg38 | 43857 | hg19 | 43857 | hg18 | 43857 | hg17 | 43857 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv699272, nssv679849, nssv678496, nssv668794, nssv687806, nssv677138, nssv669782, nssv684014 | Samples | | Known Genes | SNX14 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv516516
| Frequency | Sample Size | 2026 | Observed Gain | 1 | Observed Loss | 7 | Observed Complex | 0 | Frequency | n/a |
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