Variant DetailsVariant: esv3647324 Internal ID | 6687379 | Landmark | | Location Information | | Cytoband | 22q11.22 | Allele length | Assembly | Allele length | hg38 | 158974 | hg19 | 158994 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv16371044, essv16371054, essv16371055, essv16371019, essv16371056, essv16371026, essv16371028, essv16371052, essv16371040, essv16371050, essv16371037, essv16371042, essv16371049, essv16371043, essv16371027, essv16371025, essv16371021, essv16371041, essv16371047, essv16371033, essv16371051, essv16371053, essv16371018, essv16371024, essv16371029, essv16371031, essv16371039, essv16371023, essv16371032, essv16371036, essv16371020, essv16371030, essv16371045, essv16371048, essv16371034, essv16371046, essv16371022, essv16371057, essv16371035, essv16371038 | Samples | HG01438, NA19204, HG03111, HG02394, NA12005, HG03268, HG03380, HG03058, NA20535, NA19210, HG00557, NA20519, HG02165, NA18981, HG03382, NA11893, NA18856, HG02141, NA12827, HG00704, NA18523, HG02568, NA20534, NA18646, HG03240, HG02308, NA18950, NA20351, NA19428, NA07037, HG03557, HG02032, HG02182, HG02051, HG01479, HG03445, HG02947, HG02643, NA20772, NA20511 | Known Genes | TOP3B | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3647324
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 40 | Observed Complex | 0 | Frequency | n/a |
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