Variant DetailsVariant: esv3636116 Internal ID | 6676225 | Landmark | | Location Information | | Cytoband | 15q14 | Allele length | Assembly | Allele length | hg38 | 115591 | hg19 | 115591 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv15211048, essv15211055, essv15211081, essv15211052, essv15211060, essv15211080, essv15211074, essv15211049, essv15211057, essv15211084, essv15211061, essv15211085, essv15211078, essv15211064, essv15211069, essv15211053, essv15211051, essv15211075, essv15211045, essv15211066, essv15211077, essv15211070, essv15211054, essv15211086, essv15211062, essv15211073, essv15211082, essv15211083, essv15211050, essv15211046, essv15211076, essv15211063, essv15211056, essv15211079, essv15211047, essv15211067, essv15211071, essv15211059, essv15211065, essv15211068, essv15211058, essv15211087, essv15211072 | Samples | NA18745, HG02574, HG02628, NA19066, NA18592, HG03753, HG02061, NA20507, HG02589, NA18526, HG01694, HG01513, NA19201, HG01459, HG03604, HG02130, HG00736, HG01848, NA18964, HG03520, HG01519, HG04020, HG02882, NA19007, NA18934, NA18956, HG01882, HG02144, NA18879, NA19740, HG03024, HG02256, NA19035, HG02282, NA18535, HG01977, NA20281, HG02771, HG02974, NA18609, NA19096, HG03611, HG02465 | Known Genes | GOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3636116
| Frequency | Sample Size | 2504 | Observed Gain | 43 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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