Variant DetailsVariant: esv1003868Internal ID | 6715995 | Landmark | | Location Information | | Cytoband | 1p21.1 | Allele length | Assembly | Allele length | hg38 | 166685 | hg19 | 166685 | hg18 | 166685 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv3586624 | Samples | HuRef | Known Genes | AMY1A, AMY1B, AMY1C, AMY2A | Method | Oligo aCGH | Analysis | | Platform | Not Submitted | Comments | | Reference | Pang_et_al_2010 | Pubmed ID | 20482838 | Accession Number(s) | esv1003868
| Frequency | Sample Size | 3 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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