Gels formed by coupling two different four-arm star polymers lead to polymer networks with high strength and low spatial heterogeneity. However, like all real polymer networks, these materials contain topological defects which affect their properties. In this study, kinetic graph theory and Monte Carlo simulation are used to investigate the structure and cyclic defects formed via A-B type end-linking of symmetric tetra-arm star polymer precursors. While loops constituting of odd number of junctions are forbidden by precursor chemistry, the amount and the correlation of secondary loops are found to increase with decreasing precursor concentration. This suppresses gelation, and the delay of gel point is quantitatively predicted by the topological simulations. Furthermore, comparison with network formed with asymmetric bifunctional-tetrafunctional precursors revealed that the behavior of loops consisting of 2n junctions in the symmetric system is analogous to the behavior of loops consisting of n junctions in the asymmetrical system, suggesting analogies between chemically distinct networks.