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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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| nstd201 | nssv16297004 | copy number gain | SNP array | Probe signal intensity | No | 1 | GRCh37 (hg19) | NC_000023.10 | X | 61728816 | 155233846 | Submitted genomic | |||||||||
| nstd201 | nssv16297004 | copy number gain | SNP array | Probe signal intensity | No | 1 | GRCh37 (hg19) | NC_000023.10 | X | 61728816 | 155233846 | Submitted genomic | |||||||||
| nstd201 | nssv16297004 | copy number gain | SNP array | Probe signal intensity | No | 1 | GRCh38.p12 | NC_000023.11 | X | 62509346 | 156004181 | Remapped | 0.99989 | ||||||||
| nstd201 | nssv16297005 | copy number loss | Oligo aCGH | Probe signal intensity | No | 2 | GRCh37 (hg19) | NC_000023.10 | X | 96096220 | 155208244 | Submitted genomic | |||||||||
| nstd201 | nssv16297005 | copy number loss | Oligo aCGH | Probe signal intensity | No | 2 | GRCh37 (hg19) | NC_000023.10 | X | 96096220 | 155208244 | Submitted genomic | |||||||||
| nstd201 | nssv16297005 | copy number loss | Oligo aCGH | Probe signal intensity | No | 2 | GRCh38.p12 | NC_000023.11 | X | 96841221 | 155978579 | Remapped | 1.00043 | ||||||||
| nstd201 | nssv16297006 | copy number loss | SNP array | Probe signal intensity | No | 3 | GRCh37 (hg19) | NC_000023.10 | X | 168546 | 21870371 | Submitted genomic | |||||||||
| nstd201 | nssv16297006 | copy number loss | SNP array | Probe signal intensity | No | 3 | GRCh37 (hg19) | NC_000023.10 | X | 168546 | 21870371 | Submitted genomic | |||||||||
| nstd201 | nssv16297006 | copy number loss | SNP array | Probe signal intensity | No | 3 | GRCh38.p12 | NC_000023.11 | X | 251879 | 21852253 | Remapped | 0.99533 | ||||||||
| nstd201 | nssv16297007 | copy number loss | SNP array | Probe signal intensity | No | 3 | GRCh37 (hg19) | NC_000013.10 | 13 | 109490236 | 115107733 | Submitted genomic | |||||||||
| nstd201 | nssv16297007 | copy number loss | SNP array | Probe signal intensity | No | 3 | GRCh37 (hg19) | NC_000013.10 | 13 | 109490236 | 115107733 | Submitted genomic | |||||||||
| nstd201 | nssv16297007 | copy number loss | SNP array | Probe signal intensity | No | 3 | GRCh38.p12 | NC_000013.11 | 13 | 108837888 | 114342258 | Remapped | 0.97986 |