Variant DetailsVariant: nsv516032Internal ID | 15096639 | Landmark | | Location Information | | Cytoband | 18p11.31 | Allele length | Assembly | Allele length | hg38 | 1598 | hg19 | 1598 | hg18 | 1598 | hg17 | 1598 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv672483, nssv654777, nssv667318, nssv693512, nssv666453, nssv682463, nssv691554, nssv665823, nssv685180, nssv693761, nssv679141, nssv705273, nssv685758, nssv675856 | 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) | nsv516032
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 14 | Observed Complex | 0 | Frequency | n/a |
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