Variant DetailsVariant: nsv516152Internal ID | 15096759 | Landmark | | Location Information | | Cytoband | 18p11.31 | Allele length | Assembly | Allele length | hg38 | 13242 | hg19 | 13242 | hg18 | 13242 | hg17 | 13242 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv670650, nssv674830, nssv658068, nssv665993, nssv684930, nssv674506, nssv680346, nssv678050, nssv652553, nssv678845, nssv705961, nssv690154, nssv683590, nssv682490, nssv665122, nssv673477, nssv693693, nssv678005, nssv659268, nssv686641 | Samples | | Known Genes | DLGAP1 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv516152
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 20 | Observed Complex | 0 | Frequency | n/a |
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