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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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| nstd184 | nssv16154040 | copy number loss | MLPA | Genotyping | No | M25 | GRCh37 (hg19) | NC_000023.10 | X | 149613840 | 150156259 | Submitted genomic | |||||||||
| nstd184 | nssv16154040 | copy number loss | MLPA | Genotyping | No | M25 | GRCh37 (hg19) | NC_000023.10 | X | 149613840 | 150156259 | Submitted genomic | |||||||||
| nstd184 | nssv16154040 | copy number loss | MLPA | Genotyping | No | M25 | GRCh38.p12 | NC_000023.11 | X | 150445574 | 150987786 | Remapped | 0.99962 | ||||||||
| nstd184 | nsv4634377 | copy number variation | No | GRCh37 (hg19) | NC_000023.10 | X | 149613840 | 150156259 | Submitted genomic | ||||||||||||
| nstd184 | nsv4634377 | copy number variation | No | GRCh37 (hg19) | NC_000023.10 | X | 149613840 | 150156259 | Submitted genomic | ||||||||||||
| nstd184 | nsv4634377 | copy number variation | No | GRCh38.p12 | NC_000023.11 | X | 150445574 | 150987786 | Remapped | 0.99962 |