Variant DetailsVariant: esv3587620Internal ID | 6627921 | Landmark | | Location Information | | Cytoband | 1q22 | Allele length | Assembly | Allele length | hg38 | 23185 | hg19 | 23185 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv55e214 | Supporting Variants | essv10152192, essv10152185, essv10152175, essv10152178, essv10152179, essv10152187, essv10152184, essv10152188, essv10152182, essv10152173, essv10152177, essv10152176, essv10152193, essv10152181, essv10152195, essv10152180, essv10152174, essv10152189, essv10152186, essv10152183, essv10152194, essv10152191, essv10152190, essv10152172 | Samples | NA20298, NA18878, HG03926, HG03295, NA20756, HG03913, HG03578, NA19159, HG04185, HG03760, HG01880, HG01889, HG00404, HG02577, HG03028, NA19331, NA19334, NA20902, HG02941, HG03432, HG03097, HG01055, NA18983, HG03439 | Known Genes | GBA, GBAP1, MTX1 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3587620
| Frequency | Sample Size | 2504 | Observed Gain | 24 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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