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Warning: This build has drifted.
The coverage report for this pull request build may be inaccurate because its base commit is no longer the HEAD of its target branch.
This means it includes changes from outside the original pull request, including, potentially, unrelated coverage changes.

    • Learn more: For more information on this, see Tracking coverage changes for pull request builds.
    • Fix now: For a quick fix, rebase this PR at GitHub. Your next report should be accurate.
    • Prevent going forward: To avoid this issue with future PRs, see these Recommended CI Configurations.
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Clinical-Genomics / cg / 21674763594
83%
master: 83%

Build:
Build:
LAST BUILD BRANCH: validate-no-relationships
DEFAULT BRANCH: master
Ran 04 Feb 2026 02:15PM UTC
Jobs 1
Files 885
Run time 1min
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04 Feb 2026 02:12PM UTC coverage: 83.211%. First build
21674763594

Pull #4871

github

web-flow
Merge 854e1cba1 into 41f73d273
Pull Request #4871: DEV - Switch reference genome to hg38 for raredisease

9442 of 11347 relevant lines covered (83.21%)

2.49 hits per line

Jobs
ID Job ID Ran Files Coverage
1 21674763594.1 04 Feb 2026 02:15PM UTC 885
86.46
GitHub Action Run
Source Files on build 21674763594
  • Tree
  • List 885
  • Changed 0
  • Source Changed 0
  • Coverage Changed 0
Coverage ∆ File Lines Relevant Covered Missed Hits/Line
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  • Pull Request #4871
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