Variant DetailsVariant: nsv515998Internal ID | 15096605 | Landmark | | Location Information | | Cytoband | 7q21.13 | Allele length | Assembly | Allele length | hg38 | 127205 | hg19 | 127205 | hg18 | 127205 | hg17 | 127205 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv677433, nssv674797, nssv665640, nssv681563, nssv657362 | Samples | | Known Genes | CDK14 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv515998
| Frequency | Sample Size | 2026 | Observed Gain | 5 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|