Variant DetailsVariant: essv11306546Internal ID | 1308362 | Landmark | | Location Information | | Cytoband | 3q29 | Allele length | Assembly | Allele length | hg38 | 68378 | hg19 | 68378 |
| Variant Type | CNV loss | Copy Number | | Allele State | Heterozygous | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | esv3599276 | Supporting Variants | | Samples | HG02075 | Known Genes | PCYT1A, SLC51A, TCTEX1D2 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | essv11306546
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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