Variant DetailsVariant: nsv515627Internal ID | 15096234 | Landmark | | Location Information | | Cytoband | 10q24.31 | Allele length | Assembly | Allele length | hg38 | 19165 | hg19 | 19165 | hg18 | 19165 | hg17 | 19165 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv686756, nssv678267, nssv664153, nssv676676, nssv669368, nssv685656, nssv674074, nssv681366, nssv669143, nssv669086, nssv680693, nssv661591 | Samples | | Known Genes | FAM178A | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv515627
| Frequency | Sample Size | 2026 | Observed Gain | 10 | Observed Loss | 2 | Observed Complex | 0 | Frequency | n/a |
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