Variant DetailsVariant: esv3586181 Internal ID | 6626494 | Landmark | | Location Information | | Cytoband | 1p32.1 | Allele length | Assembly | Allele length | hg38 | 825 | hg19 | 825 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv9942953, essv9942960, essv9942965, essv9943020, essv9943016, essv9942989, essv9943007, essv9942994, essv9943005, essv9943011, essv9942987, essv9942951, essv9943010, essv9942968, essv9943019, essv9942956, essv9943000, essv9942945, essv9942995, essv9942996, essv9942969, essv9942961, essv9942944, essv9942967, essv9942991, essv9943018, essv9943004, essv9943006, essv9943009, essv9942988, essv9942984, essv9942976, essv9943015, essv9942947, essv9943014, essv9942971, essv9943001, essv9943003, essv9942966, essv9942970, essv9943002, essv9943017, essv9942958, essv9942946, essv9942973, essv9942974, essv9942992, essv9942952, essv9942957, essv9942972, essv9943008, essv9942986, essv9942949, essv9942977, essv9942983, essv9942982, essv9942948, essv9942959, essv9942954, essv9943013, essv9942997, essv9942979, essv9942999, essv9942998, essv9942975, essv9942990, essv9942955, essv9942981, essv9942950, essv9942978, essv9942993, essv9942963, essv9942964, essv9942962, essv9943012, essv9942985, essv9942980 | Samples | HG01443, HG03548, NA19914, HG02973, HG03449, HG02012, NA19350, NA19092, HG03297, HG02536, NA19443, NA20356, HG03478, NA19107, HG03095, NA19171, HG03436, HG02485, NA18498, NA19782, NA20291, HG02561, HG03212, NA20340, HG02885, NA19159, NA18520, NA19209, HG03583, HG03369, HG02879, HG02479, HG02009, HG03343, HG01136, NA18934, NA18933, HG01095, NA19043, HG02322, HG02450, HG02144, NA18910, NA18871, HG02555, HG03085, HG02429, HG03397, HG02881, HG01130, HG03451, HG03391, HG03354, HG02772, HG02255, HG02807, NA19834, NA19149, NA20276, NA18865, NA19439, HG02580, NA18501, HG02974, HG03025, HG02938, HG01781, HG03401, HG02051, HG03445, HG02947, NA19129, NA19312, HG02851, NA18522, HG02629, HG03118 | Known Genes | FGGY | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3586181
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 77 | Observed Complex | 0 | Frequency | n/a |
|
|