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Data loss owing to missing data was less than 1%.
Few missing data was also a strength.
The rate of missing data was 2.4%.
The missing data was handled with pairwise deletion.
Where it was possible, without risking bias, missing data was imputed using standard methodologies [25].
For each sample, a window of 15 SNPs without missing data was used for genotyping calling.
Imputation of missing data was not necessary and the cases were removed.
As noted above, missing data was replaced using the last observation carried forward method.
No imputation of missing data was conducted.
Exclusion because of missing data was < 1%.
No imputation of missing data was used.
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