Variant DetailsVariant: nsv517541Internal ID | 15098148 | Landmark | | Location Information | | Cytoband | 15q15.1 | Allele length | Assembly | Allele length | hg38 | 38360 | hg19 | 38360 | hg18 | 38360 | hg17 | 38360 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv692799, nssv660429, nssv656052, nssv677810, nssv678807, nssv652307, nssv688330, nssv668844, nssv692537, nssv669798, nssv671568, nssv667247, nssv685331 | Samples | | Known Genes | ANKRD63, PAK6, PLCB2 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv517541
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 13 | Observed Complex | 0 | Frequency | n/a |
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