Variant DetailsVariant: esv3587621Internal ID | 6627922 | 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 | essv10152206, essv10152198, essv10152205, essv10152209, essv10152207, essv10152202, essv10152218, essv10152200, essv10152199, essv10152211, essv10152212, essv10152217, essv10152196, essv10152216, essv10152213, essv10152215, essv10152214, essv10152208, essv10152203, essv10152210, essv10152204, essv10152201, essv10152197 | Samples | NA18917, HG02891, NA19393, NA19190, HG03478, HG03199, HG03095, HG03485, HG03479, NA20340, NA19235, NA19172, NA19317, HG02554, HG00598, HG03123, NA19031, NA19428, NA20348, NA19711, HG02947, NA19129, NA19312 | Known Genes | GBA, GBAP1, MTX1 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3587621
| Frequency | Sample Size | 2504 | Observed Gain | 23 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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