Variant DetailsVariant: esv3586684 Internal ID | 6626994 | Landmark | | Location Information | | Cytoband | 1p22.3 | Allele length | Assembly | Allele length | hg38 | 25684 | hg19 | 25684 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv32e214 | Supporting Variants | essv10007050, essv10007047, essv10007045, essv10007055, essv10007034, essv10007060, essv10007030, essv10007056, essv10007063, essv10007037, essv10007036, essv10007054, essv10007031, essv10007024, essv10007042, essv10007038, essv10007041, essv10007048, essv10007044, essv10007026, essv10007052, essv10007059, essv10007035, essv10007057, essv10007046, essv10007062, essv10007029, essv10007023, essv10007033, essv10007025, essv10007061, essv10007028, essv10007022, essv10007032, essv10007040, essv10007053, essv10007027, essv10007058, essv10007039, essv10007043, essv10007051, essv10007049 | Samples | HG02610, HG01521, HG01356, HG03378, HG01303, NA19914, HG02433, HG02012, HG03100, HG02589, NA18519, HG02811, HG03091, NA18923, HG03485, NA20287, HG01668, HG03079, NA19404, HG03352, HG02502, NA19209, HG02716, HG03343, HG03120, NA12342, NA19175, NA19114, NA19042, NA19318, NA19625, HG02255, HG02557, HG03240, HG03127, NA21095, NA19376, HG03157, NA19472, HG03162, HG03129, HG03439 | Known Genes | DDAH1 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3586684
| Frequency | Sample Size | 2504 | Observed Gain | 42 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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