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| Study ID | Variant ID | Variant Region type | Variant Call type | Sampleset ID | Method | Analysis ID | Validation | Variant samples | Subject phenotype | Clinical Interpretation | Assembly | Accession | Chr | Outer-Start | Start | Inner-Start | Inner-End | End | Outer-End | Placement Type | Remap Score |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| estd186 | esv1791726 | copy number variation | Yes | GRCh37.p13 | NC_000001.10 | 1 | 6848878 | 6854451 | 6903599 | 6912597 | Remapped | 1 | |||||||||
| estd186 | esv1791726 | copy number variation | Yes | GRCh37.p13 | NC_000001.10 | 1 | 6848878 | 6854451 | 6903599 | 6912597 | Remapped | 1 | |||||||||
| estd186 | esv1791726 | copy number variation | Yes | GRCh38.p12 | NC_000001.11 | 1 | 6788818 | 6794391 | 6843539 | 6852537 | Remapped | 1 | |||||||||
| estd186 | esv1791726 | copy number variation | Yes | NCBI36 (hg18) | NC_000001.9 | 1 | 6771465 | 6777038 | 6826186 | 6835184 | Submitted genomic | ||||||||||
| estd186 | esv1791727 | copy number variation | Yes | GRCh37.p13 | NC_000001.10 | 1 | 6941117 | 6959785 | 7499528 | 7525200 | Remapped | 1 | |||||||||
| estd186 | esv1791727 | copy number variation | Yes | GRCh37.p13 | NC_000001.10 | 1 | 6941117 | 6959785 | 7499528 | 7525200 | Remapped | 1 | |||||||||
| estd186 | esv1791727 | copy number variation | Yes | GRCh38.p12 | NC_000001.11 | 1 | 6881057 | 6881057 | 7465140 | 7465140 | Remapped | 1 | |||||||||
| estd186 | esv1791727 | copy number variation | Yes | NCBI36 (hg18) | NC_000001.9 | 1 | 6863704 | 6882372 | 7422115 | 7447787 | Submitted genomic | ||||||||||
| estd186 | esv1791728 | copy number variation | Yes | GRCh37.p13 | NC_000001.10 | 1 | 7101726 | 7119268 | 7211189 | 7256822 | Remapped | 1 | |||||||||
| estd186 | esv1791728 | copy number variation | Yes | GRCh37.p13 | NC_000001.10 | 1 | 7101726 | 7119268 | 7211189 | 7256822 | Remapped | 1 | |||||||||
| estd186 | esv1791728 | copy number variation | Yes | GRCh38.p12 | NC_000001.11 | 1 | 7041666 | 7059208 | 7151129 | 7196762 | Remapped | 1 | |||||||||
| estd186 | esv1791728 | copy number variation | Yes | NCBI36 (hg18) | NC_000001.9 | 1 | 7024313 | 7041855 | 7133776 | 7179409 | Submitted genomic |