Variant DetailsVariant: esv3643462Internal ID | 6683536 | Landmark | | Location Information | | Cytoband | 19p13.3 | Allele length | Assembly | Allele length | hg38 | 1542 | hg19 | 1542 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv15974570, essv15974573, essv15974576, essv15974571, essv15974574, essv15974575, essv15974572, essv15974569 | Samples | NA20899, HG03895, HG03950, HG03604, NA21112, HG03238, HG03703, HG03611 | Known Genes | NFIC | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3643462
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 8 | Observed Complex | 0 | Frequency | n/a |
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