Please click here to confirm download.
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| nstd222 | nssv17977124 | copy number loss | Sequencing | Sequence alignment | No | LLDD006.3 | GRCh37.p13 | NC_000016.9 | 16 | 85986306 | 86727693 | Remapped | 1 | ||||||||
| nstd222 | nssv17977124 | copy number loss | Sequencing | Sequence alignment | No | LLDD006.3 | GRCh37.p13 | NC_000016.9 | 16 | 85986306 | 86727693 | Remapped | 1 | ||||||||
| nstd222 | nssv17977124 | copy number loss | Sequencing | Sequence alignment | No | LLDD006.3 | GRCh38 (hg38) | NC_000016.10 | 16 | 85952700 | 86694087 | Submitted genomic | |||||||||
| nstd222 | nssv17977124 | copy number loss | Sequencing | Sequence alignment | No | LLDD006.3 | GRCh38 (hg38) | NC_000016.10 | 16 | 85952700 | 86694087 | Submitted genomic |