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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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| nstd228 | nssv18786564 | copy number loss | SNP array | SNP genotyping analysis | Yes | 1 | GRCh37 (hg19) | NC_000004.11 | 4 | 171508974 | 171509635 | 190957473 | Submitted genomic | ||||||||
| nstd228 | nssv18786564 | copy number loss | SNP array | SNP genotyping analysis | Yes | 1 | GRCh37 (hg19) | NC_000004.11 | 4 | 171508974 | 171509635 | 190957473 | Submitted genomic | ||||||||
| nstd228 | nssv18786564 | copy number loss | SNP array | SNP genotyping analysis | Yes | 1 | GRCh38.p12 | NC_000004.12 | 4 | 170587823 | 170587823 | 190036318 | Remapped | 1 | |||||||
| nstd228 | nssv18786565 | copy number gain | SNP array | SNP genotyping analysis | Yes | 1 | GRCh37 (hg19) | NC_000010.10 | 10 | 100026 | 5313662 | 5331694 | Submitted genomic | ||||||||
| nstd228 | nssv18786565 | copy number gain | SNP array | SNP genotyping analysis | Yes | 1 | GRCh37 (hg19) | NC_000010.10 | 10 | 100026 | 5313662 | 5331694 | Submitted genomic | ||||||||
| nstd228 | nssv18786565 | copy number gain | SNP array | SNP genotyping analysis | Yes | 1 | GRCh38.p12 | NC_000010.11 | 10 | 54086 | 5289731 | 5289731 | Remapped | 1.00076 | |||||||
| nstd228 | nsv7093619 | copy number variation | Yes | GRCh37 (hg19) | NC_000004.11 | 4 | 171508974 | 171509635 | 190957473 | Submitted genomic | |||||||||||
| nstd228 | nsv7093619 | copy number variation | Yes | GRCh37 (hg19) | NC_000004.11 | 4 | 171508974 | 171509635 | 190957473 | Submitted genomic | |||||||||||
| nstd228 | nsv7093619 | copy number variation | Yes | GRCh38.p12 | NC_000004.12 | 4 | 170587823 | 170587823 | 190036318 | Remapped | 1 | ||||||||||
| nstd228 | nsv7093620 | copy number variation | Yes | GRCh37 (hg19) | NC_000010.10 | 10 | 100026 | 5313662 | 5331694 | Submitted genomic | |||||||||||
| nstd228 | nsv7093620 | copy number variation | Yes | GRCh37 (hg19) | NC_000010.10 | 10 | 100026 | 5313662 | 5331694 | Submitted genomic | |||||||||||
| nstd228 | nsv7093620 | copy number variation | Yes | GRCh38.p12 | NC_000010.11 | 10 | 54086 | 5289731 | 5289731 | Remapped | 1.00076 |