Variant DetailsVariant: esv3628003Internal ID | 6668147 | Landmark | | Location Information | | Cytoband | 11q24.2 | Allele length | Assembly | Allele length | hg38 | 2857 | hg19 | 2857 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv14302950, essv14302957, essv14302955, essv14302959, essv14302951, essv14302961, essv14302958, essv14302953, essv14302963, essv14302954, essv14302962, essv14302964, essv14302952, essv14302960, essv14302956, essv14302949 | Samples | HG03298, NA19916, HG02111, HG03268, NA19024, NA19235, HG02442, HG02508, HG03311, HG03117, NA19360, HG02558, NA20348, HG02974, HG03445, NA19346 | Known Genes | DCPS | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3628003
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 16 | Observed Complex | 0 | Frequency | n/a |
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