Variant DetailsVariant: nsv517661Internal ID | 15098268 | Landmark | | Location Information | | Cytoband | 9q34.11 | Allele length | Assembly | Allele length | hg38 | 24692 | hg19 | 24692 | hg18 | 24692 | hg17 | 24692 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv497n21 | Supporting Variants | nssv669878, nssv688458, nssv684661, nssv672941, nssv666230, nssv652736, nssv674921, nssv654584, nssv662036, nssv655767, nssv693953, nssv670671, nssv672101, nssv664076, nssv682101, nssv686732, nssv670409, nssv671483 | Samples | | Known Genes | AK1, ST6GALNAC6 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv517661
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 18 | Observed Complex | 0 | Frequency | n/a |
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