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Summary of unique non-SNP VCF entries in bi-allelic indel array resources (Mills et al., 2011) and dbSNP 141, before/after normalization
| Counts/% of variants | Indel array | dbSNP 141 |
|---|---|---|
| Number before/after normalization | 9996/8904 | 6 367 920/6 077 962 |
| % 1000G overlaps (before/after) | 49%/81% | 26%/28% |
| % Need normalization | 40% | 14% |
| % Redundant | 11% | 4.6% |
