Variant DetailsVariant: nsv516224Internal ID | 15096831 | Landmark | | Location Information | | Cytoband | 11q23.1 | Allele length | Assembly | Allele length | hg38 | 363 | hg19 | 363 | hg18 | 363 | hg17 | 363 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv681966, nssv670225, nssv662805, nssv657979, nssv673470, nssv666919, nssv691533, nssv662460, nssv658868, nssv686239 | Samples | | Known Genes | NCAM1 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv516224
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 10 | Observed Complex | 0 | Frequency | n/a |
|
|