Variant DetailsVariant: nsv606774Internal ID | 16047497 | Landmark | | Location Information | | Cytoband | 7p13 | Allele length | Assembly | Allele length | hg38 | 694 | hg19 | 694 | hg18 | 694 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv11305n54 | Supporting Variants | nssv1083383, nssv1083385, nssv1083387, nssv1083386, nssv1083389, nssv1083391, nssv1083388, nssv1083390, nssv1083382, nssv1083392, nssv1083384 | Samples | | Known Genes | CAMK2B | 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) | nsv606774
| Frequency | Sample Size | 17421 | Observed Gain | 11 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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