Variant DetailsVariant: nssv1847773Internal ID | 17448337 | Landmark | | Location Information | | Cytoband | 10q11.22 | Allele length | Assembly | Allele length | hg38 | 72082 | hg19 | 72085 | hg18 | 72085 |
| Variant Type | CNV duplication | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv947974 | Supporting Variants | | Samples | HGDP00778 | Known Genes | CTGLF12P, FAM25C, FAM25G | Method | Sequencing | Analysis | lineage specific fixed duplications | Platform | Not reported | Comments | lineage specific duplication - fixed_Pab-Ppy-Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde | Reference | Sudmant_et_al_2013 | Pubmed ID | 23825009 | Accession Number(s) | nssv1847773
| Frequency | Sample Size | 10 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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