Variant DetailsVariant: esv1063774Internal ID | 11880213 | Landmark | | Location Information | | Cytoband | 11p15.2 | Allele length | Assembly | Allele length | hg38 | 1063 | hg19 | 1063 | hg18 | 1063 |
| Variant Type | CNV insertion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv4241462 | Samples | HuRef | Known Genes | PDE3B | Method | Sequencing | Analysis | | Platform | Sanger Sequencing | Comments | | Reference | Levy_et_al_2007 | Pubmed ID | 17803354 | Accession Number(s) | esv1063774
| Frequency | Sample Size | 2 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|