Variant DetailsVariant: nsv551834Internal ID | 15992557 | Landmark | | Location Information | | Cytoband | 10q23.31 | Allele length | Assembly | Allele length | hg38 | 809 | hg19 | 809 | hg18 | 809 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv1333n54 | Supporting Variants | nssv753192, nssv753191, nssv753187, nssv753183, nssv753184, nssv753186, nssv753180, nssv753181, nssv753189, nssv753190, nssv753182, nssv753193, nssv753179, nssv753178, nssv753177, nssv753185, nssv753188 | Samples | | Known Genes | PTEN | Method | SNP array | Analysis | Illumina SNP array copy number analysis | Platform | Not reported | Comments | | Reference | Cooper_et_al_2011 | Pubmed ID | 21841781 | Accession Number(s) | nsv551834
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 17 | Observed Complex | 0 | Frequency | n/a |
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