| CNVs | Copy number variants |
| InDels | Insertions and deletions |
| LGRs | Large genomic rearrangements |
| RSF | Russian Science Foundation |
| SNVs | Single Nucleotide Variants |
| SRA | Sequence Read Archive |
| VAF | Variant allele frequency |
| CNVs | Copy number variants |
| InDels | Insertions and deletions |
| LGRs | Large genomic rearrangements |
| RSF | Russian Science Foundation |
| SNVs | Single Nucleotide Variants |
| SRA | Sequence Read Archive |
| VAF | Variant allele frequency |