Variant DetailsVariant: nsv517387Internal ID | 15097994 | Landmark | | Location Information | | Cytoband | 5p13.3 | Allele length | Assembly | Allele length | hg38 | 87941 | hg19 | 87941 | hg18 | 87941 | hg17 | 87941 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv686508, nssv692921, nssv692617, nssv657727, nssv673833, nssv679681, nssv683810, nssv683367, nssv666703, nssv664903, nssv659254, nssv689430, nssv651873, nssv675818, nssv651993, nssv665343, nssv670293, nssv682711, nssv676452, nssv673070, nssv670079, nssv689249, nssv685781, nssv677310, nssv665298 | Samples | | Known Genes | GOLPH3, PDZD2 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv517387
| Frequency | Sample Size | 2026 | Observed Gain | 25 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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