Variant DetailsVariant: nsv517357Internal ID | 15097964 | Landmark | | Location Information | | Cytoband | 11p11.2 | Allele length | Assembly | Allele length | hg38 | 21008 | hg19 | 21008 | hg18 | 21008 | hg17 | 21008 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv67n21 | Supporting Variants | nssv651808, nssv673390, nssv697802, nssv669788, nssv656695, nssv679889, nssv665488, nssv673303, nssv671368, nssv705210, nssv656877, nssv687101, nssv663276 | Samples | | Known Genes | ALX4 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv517357
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 13 | Observed Complex | 0 | Frequency | n/a |
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