Variant DetailsVariant: esv2871568Internal ID | 10544548 | Landmark | | Location Information | | Cytoband | 12p13.31 | Allele length | Assembly | Allele length | hg38 | 12001 | hg19 | 12001 |
| Variant Type | CNV duplication | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv7141135 | Samples | HuRef | Known Genes | FAM86FP, FAM90A1 | Method | Sequencing | Analysis | | Platform | Complete Genomics | Comments | | Reference | Pang_et_al_2013b | Pubmed ID | 24192839 | Accession Number(s) | esv2871568
| Frequency | Sample Size | 1 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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