Variant DetailsVariant: nsv517665Internal ID | 15098272 | Landmark | | Location Information | | Cytoband | 16q23.3 | Allele length | Assembly | Allele length | hg38 | 137 | hg19 | 137 | hg18 | 137 | hg17 | 137 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv675668, nssv663395, nssv677237, nssv667747, nssv686180, nssv688765, nssv688881, nssv663240, nssv666049, nssv660381, nssv676177, nssv664979, nssv652766, nssv671933, nssv690445, nssv666076, nssv681160, nssv688046 | Samples | | Known Genes | CDH13 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv517665
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 18 | Observed Complex | 0 | Frequency | n/a |
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